| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:144170575-144170907 | Common:7; Rare:106 | ||||
| chr5:144205160-144205530 | Rare:73 | ||||
| chr5:145835296-145835525 | Common:3; Rare:54 | ||||
| chr5:145936280-145936760 | Common:3; Rare:93 | ||||
| chr5:146182492-146182957 | Common:4; Rare:134 | ||||
| chr5:146203403-146203676 | Common:2; Rare:88 | ||||
| chr5:146203797-146204129 | Common:1; Rare:102 | ||||
| chr5:146446900-146447392 | Common:3; Rare:119 | ||||
| chr5:146447521-146447921 | Common:6; Rare:167 | ||||
| chr5:146878550-146879040 | Common:5; Rare:115; Clinvar (benign):1 | ||||
| chr5:147084690-147085060 | Rare:72 | ||||
| chr5:147453652-147453884 | Common:6; Rare:65 | ||||
| chr5:147453912-147454069 | Common:1; Rare:38 | ||||
| chr5:147508947-147509116 | Common:1; Rare:30 | ||||
| chr5:147509939-147510064 | Rare:24 |